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首页> 外文期刊>Chemico-biological interactions >Cytotoxic effects of new trans-2,4-diaryl-r-3-methyl-1,2,3,4-tetrahydroquinolines and their interaction with antitumoral drugs gemcitabine and paclitaxel on cellular lines of human breast cancer.
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Cytotoxic effects of new trans-2,4-diaryl-r-3-methyl-1,2,3,4-tetrahydroquinolines and their interaction with antitumoral drugs gemcitabine and paclitaxel on cellular lines of human breast cancer.

机译:新的反式2,4-二芳基-r-3-甲基-1,2,3,4-四氢喹啉的细胞毒性作用及其与抗肿瘤药吉西他滨和紫杉醇的相互作用对人乳腺癌细胞的影响。

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摘要

Two tetrahydroquinoline compounds, called DM8 and DM12, from a new series of the cis-2,4-diaryl-r-3-methyl-1,2,3,4-tetrahydroquinolines, were selected for cytotoxic effects studies on cellular lines of human breast cancer. The synergistic, additive and antagonistic effects in combination of these compounds with anticancer drugs, such as paclitaxel and gemcitabine, were studied. The isobolograms and their analysis demonstrated models of synergism, additivity and antagonism of these tetrahydroquinolines in the presence of paclitaxel and gemcitabine. Results showed that compounds DM8 and DM12 individually induced growth inhibition on breast cancer cell lines MCF-7 and SKBR3, and the addition of paclitaxel and gemcitabine intensified their cytotoxic activity on both cell lines at conc. below 1 mug/mL. During these studies the compound DM12 was identified as new, perspective and safe agent for adjuvant therapy.
机译:从新的顺式-2,4-二芳基-r-3-甲基-1,2,3,4-四氢喹啉系列中选择了两种称为DM8和DM12的四氢喹啉化合物,用于研究人类细胞系的细胞毒性作用乳腺癌。研究了这些化合物与抗癌药(例如紫杉醇和吉西他滨)的协同,加和和拮抗作用。等效线图及其分析证明了在紫杉醇和吉西他滨存在下这些四氢喹啉的协同,加和和拮抗作用模型。结果表明,化合物DM8和DM12分别诱导对乳腺癌细胞MCF-7和SKBR3的生长抑制,并且紫杉醇和吉西他滨的加入在相同浓度下增强了它们对两种细胞的细胞毒活性。低于1杯/毫升。在这些研究中,化合物DM12被确定为辅助治疗的新型,安全的观点。

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